Canonical Allele Identifier: CA374111862

Gene: PTCH1

Linked Data

• dbSNP Id: rs2136632049
• gnomAD v4: 9-95453584-C-T
• MyVariant Identifiers: chr9:g.98215866C>T (hg19) ; chr9:g.95453584C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95453584C>T , CM000671.2:g.95453584C>T	GRCh38
NC_000009.11:g.98215866C>T , CM000671.1:g.98215866C>T	GRCh37
NC_000009.10:g.97255687C>T	NCBI36
NG_007664.1:g.68382G>A , LRG_515:g.68382G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711046.1:c.3145G>A	ENSP00000518556.1:p.Ala1049Thr
ENST00000437951.6:c.3340G>A MANE Plus Clinical	ENSP00000389744.2:p.Ala1114Thr
ENST00000690194.1:c.*1651G>A	ENSP00000509379.1:n.*1651G>A
ENST00000692981.1:c.2890G>A	ENSP00000510238.1:p.Ala964Thr
ENST00000693534.1:n.674G>A
ENST00000331920.11:c.3343G>A MANE Select	ENSP00000332353.6:p.Ala1115Thr
ENST00000331920.10:c.3343G>A	ENSP00000332353.6:p.Ala1115Thr
ENST00000375274.6:c.3340G>A	ENSP00000364423.2:p.Ala1114Thr
ENST00000375290.6:c.3112G>A	ENSP00000364439.2:n.3112G>A
ENST00000418258.5:c.2890G>A	ENSP00000396135.1:p.Ala964Thr
ENST00000421141.5:c.2890G>A	ENSP00000399981.1:p.Ala964Thr
ENST00000429896.6:c.2890G>A	ENSP00000414823.2:p.Ala964Thr
ENST00000430669.6:c.3145G>A	ENSP00000410287.2:p.Ala1049Thr
ENST00000437951.5:c.3145G>A	ENSP00000389744.1:p.Ala1049Thr
NM_000264.3:c.3343G>A , LRG_515t1:c.3343G>A	NP_000255.2:p.Ala1115Thr
NM_001083602.1:c.3145G>A , LRG_515t2:c.3145G>A	NP_001077071.1:p.Ala1049Thr
NM_001083603.1:c.3340G>A	NP_001077072.1:p.Ala1114Thr
NM_001083604.1:c.2890G>A	NP_001077073.1:p.Ala964Thr
NM_001083605.1:c.2890G>A	NP_001077074.1:p.Ala964Thr
NM_001083606.1:c.2890G>A	NP_001077075.1:p.Ala964Thr
NM_001083607.1:c.2890G>A	NP_001077076.1:p.Ala964Thr
XM_005252102.2:c.2890G>A	XP_005252159.1:p.Ala964Thr
XM_011518868.1:c.3187G>A	XP_011517170.1:p.Ala1063Thr
XM_011518869.1:c.2890G>A	XP_011517171.1:p.Ala964Thr
XM_011518870.1:c.2890G>A	XP_011517172.1:p.Ala964Thr
XM_011518871.1:c.2890G>A	XP_011517173.1:p.Ala964Thr
XM_011518872.1:c.2890G>A	XP_011517174.1:p.Ala964Thr
XM_011518873.1:c.2503G>A	XP_011517175.1:p.Ala835Thr
XM_011518874.1:c.3343G>A	XP_011517176.1:p.Ala1115Thr
NM_000264.4:c.3343G>A	NP_000255.2:p.Ala1115Thr
NM_001083602.2:c.3145G>A	NP_001077071.1:p.Ala1049Thr
NM_001083603.2:c.3340G>A	NP_001077072.1:p.Ala1114Thr
NM_001083604.2:c.2890G>A	NP_001077073.1:p.Ala964Thr
NM_001083605.2:c.2890G>A	NP_001077074.1:p.Ala964Thr
NM_001083606.2:c.2890G>A	NP_001077075.1:p.Ala964Thr
NM_001083607.2:c.2890G>A	NP_001077076.1:p.Ala964Thr
NM_001354918.1:c.3187G>A	NP_001341847.1:p.Ala1063Thr
NR_149061.1:n.3365G>A
NM_000264.5:c.3343G>A MANE Select	NP_000255.2:p.Ala1115Thr
NM_001083606.3:c.2890G>A	NP_001077075.1:p.Ala964Thr
NM_001354918.2:c.3187G>A	NP_001341847.1:p.Ala1063Thr
NR_149061.2:n.4082G>A
NM_001083602.3:c.3145G>A	NP_001077071.1:p.Ala1049Thr
NM_001083603.3:c.3340G>A MANE Plus Clinical	NP_001077072.1:p.Ala1114Thr
NM_001083604.3:c.2890G>A	NP_001077073.1:p.Ala964Thr
NM_001083605.3:c.2890G>A	NP_001077074.1:p.Ala964Thr
NM_001083607.3:c.2890G>A	NP_001077076.1:p.Ala964Thr